Canonical Allele Identifier: CA346755008

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 1515818
• ClinVar RCV Id: RCV002048625 ; RCV002425426
• dbSNP Id: rs2104415318
• MyVariant Identifiers: chr2:g.48027738A>G (hg19) ; chr2:g.47800599A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47800599A>G , CM000664.2:g.47800599A>G	GRCh38
NC_000002.11:g.48027738A>G , CM000664.1:g.48027738A>G	GRCh37
NC_000002.10:g.47881242A>G	NCBI36
NG_007111.1:g.22453A>G , LRG_219:g.22453A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2319A>G (MSH6)	ENSP00000406248.2:p.Ile773Met
ENST00000420813.6:c.2319A>G (MSH6)	ENSP00000390382.2:p.Ile773Met
ENST00000455383.6:c.2319A>G (MSH6)	ENSP00000397484.2:p.Ile773Met
ENST00000700004.2:c.2616A>G (MSH6)	ENSP00000514752.2:p.Ile872Met
ENST00000699999.1:n.2700A>G (MSH6)
ENST00000700000.1:c.1606+1010A>G (MSH6)	ENSP00000514749.1:n.1606+1010A>G
ENST00000700002.1:c.2622A>G (MSH6)	ENSP00000514750.1:p.Ile874Met
ENST00000700003.1:c.628-2821A>G (MSH6)	ENSP00000514751.1:n.628-2821A>G
ENST00000700004.1:c.1773A>G (MSH6)	ENSP00000514752.1:p.Ile591Met
ENST00000234420.11:c.2616A>G (MSH6) MANE Select	ENSP00000234420.5:p.Ile872Met
ENST00000540021.6:c.2226A>G (MSH6)	ENSP00000446475.1:p.Ile742Met
ENST00000652107.1:c.2319A>G (MSH6)	ENSP00000498629.1:p.Ile773Met
ENST00000673637.1:c.2319A>G (MSH6)	ENSP00000501310.1:p.Ile773Met
ENST00000234420.9:c.2616A>G (MSH6)	ENSP00000234420.4:p.Ile872Met
ENST00000405808.5:c.169+7596T>C (FBXO11)	ENSP00000385127.1:n.169+7596T>C
ENST00000434234.5:c.*124+7395T>C (FBXO11)	ENSP00000402692.1:n.*124+7395T>C
ENST00000445503.5:c.*1963A>G (MSH6)	ENSP00000405294.1:n.*1963A>G
ENST00000538136.1:c.1710A>G (MSH6)	ENSP00000438580.1:p.Ile570Met
ENST00000540021.5:c.2226A>G (MSH6)	ENSP00000446475.1:p.Ile742Met
ENST00000614496.4:c.1710A>G (MSH6)	ENSP00000477844.1:p.Ile570Met
ENST00000616033.4:c.2613A>G (MSH6)	ENSP00000480261.1:p.Ile871Met
ENST00000622629.4:c.-481A>G (MSH6)	ENSP00000482078.1:n.-481A>G
NM_000179.2:c.2616A>G , LRG_219t1:c.2616A>G (MSH6)	NP_000170.1:p.Ile872Met
NM_001281492.1:c.2226A>G (MSH6)	NP_001268421.1:p.Ile742Met
NM_001281493.1:c.1710A>G (MSH6)	NP_001268422.1:p.Ile570Met
NM_001281494.1:c.1710A>G (MSH6)	NP_001268423.1:p.Ile570Met
XM_005264271.1:c.2319A>G (MSH6)	XP_005264328.1:p.Ile773Met
XM_011532798.1:c.2433A>G (MSH6)	XP_011531100.1:p.Ile811Met
XM_011532799.1:c.2319A>G (MSH6)	XP_011531101.1:p.Ile773Met
XM_011532800.1:c.2319A>G (MSH6)	XP_011531102.1:p.Ile773Met
XM_024452819.1:c.2616A>G (MSH6)	XP_024308587.1:p.Ile872Met
XM_024452820.1:c.2433A>G (MSH6)	XP_024308588.1:p.Ile811Met
XM_024452821.1:c.2319A>G (MSH6)	XP_024308589.1:p.Ile773Met
XM_024452822.1:c.1710A>G (MSH6)	XP_024308590.1:p.Ile570Met
NM_000179.3:c.2616A>G (MSH6) MANE Select	NP_000170.1:p.Ile872Met
NM_001281492.2:c.2226A>G (MSH6)	NP_001268421.1:p.Ile742Met
NM_001281493.2:c.1710A>G (MSH6)	NP_001268422.1:p.Ile570Met
NM_001281494.2:c.1710A>G (MSH6)	NP_001268423.1:p.Ile570Met